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GB/T 36815-2018 English PDF

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GB/T 36815-2018: Detection and identification of Diaporthe vaccinii Shear
Status: Valid
Standard IDUSDBUY PDFLead-DaysStandard Title (Description)Status
GB/T 36815-2018359 Add to Cart 4 days Detection and identification of Diaporthe vaccinii Shear Valid

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Basic data

Standard ID: GB/T 36815-2018 (GB/T36815-2018)
Description (Translated English): Detection and identification of Diaporthe vaccinii Shear
Sector / Industry: National Standard (Recommended)
Classification of Chinese Standard: B16
Classification of International Standard: 65.020.01
Word Count Estimation: 18,164
Date of Issue: 2018-09-17
Date of Implementation: 2019-04-01
Regulation (derived from): National Standard Announcement No. 11 of 2018
Issuing agency(ies): State Administration for Market Regulation, China National Standardization Administration

GB/T 36815-2018: Detection and identification of Diaporthe vaccinii Shear

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Detection and identification of Diaporthe vaccinii Shear ICS 65.020.01 B16 National Standards of People's Republic of China Method for quarantine and identification of blueberry rot Published on.2018-09-17 Implementation of.2019-04-01 State market supervision and administration China National Standardization Administration issued

Foreword

This standard was drafted in accordance with the rules given in GB/T 1.1-2009. This standard is proposed and managed by the National Technical Committee for Phytosanitary Standardization (SAC/TC271). This standard was drafted. Tianjin Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China. The main drafters of this standard. Luo Jiafeng, Cui Tiejun, Liu Yueting, Zhang Ying, Huang Guoming, Liao Fang. Method for quarantine and identification of blueberry rot

1 Scope

This standard specifies the isolation culture, pathogenicity determination and molecular biological detection methods of blueberry fruit rot. This standard is applicable to the quarantine and identification of blueberry fruit rot fungi in host seedlings, plants and fruits of blueberry fruit rot.

2 Basic information of Raspberry rot

Chinese name. Blueberry fruit rot Scientific name. DiaporthevacciniiShear Asexual name. PhomopsisvacciniiShearN.E.Stevens English name. fruitrotofblueberry, Phomopsiscankerofblueberry, uprightdiebackofcranberry Classification status. Diaporthevaccinii Shear belongs to fungi (Fungi), Ascomycota, Ascomycetes, Diaporthales, Diapothaceae, Diaporthe. Route of transmission. The pathogens rely on the seedlings and fruits for long-distance transmission. See Appendix A for additional information on Raspberry rot.

3 Principle of the method

Pathogenic bacteria, isolation and culture traits, morphological characteristics, pathogenicity determination (see Appendix A, Appendix B, Appendix C) and ITS1/ The results of ITS4 nucleic acid sequence alignment were used as the basis for quarantine identification of blueberry fruit rot.

4 instruments and main reagents

4.1 Apparatus 4.1.1 Instruments Stereo microscope, biological microscope, ultra-clean workbench, biological incubator, electronic balance, autoclave, conventional refrigerator (-20 ° C), PCR amplification instrument, electrophoresis instrument, gel imager, high speed refrigerated centrifuge, constant temperature water bath. 4.1.2 Appliances Sterilized culture dish (diameter 90mm~100mm), triangle bottle, tweezers, surgical scissors, scalpel, inoculation needle, disposable syringe (1mL), cotton yarn, absorbent cotton, alcohol lamp, plastic mortar, adjustable micro sampler. 4.2 Primary reagents Ethylenediaminetetraacetic acid (EDTA), sodium dodecyl sulfate (SDS), Tris-HCl, chloroform, isoamyl alcohol, chloroform, ethanol, potassium chloride, Molecular biological reagents such as magnesium chloride, proteinase K, primers ITS1/ITS4, Taq polymerase, or plant tissue and fungal genome extraction The kit extracts DNA. Glucose, agar, penicillin, streptomycin, lactic acid, 2.0% sodium hypochlorite (NaClO). Acid potato glucose medium (APDA, pH 5.0~6.0), APDA selective medium (see Appendix D for preparation methods).
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